Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
Titel:
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
Auteur:
Paznekas, William A. Boyadjiev, Simeon A. Shapiro, Robert E. Daniels, Otto Wollnik, Bernd Keegan, Catherine E. Innis, Jeffrey W. Dinulos, Mary Beth Christian, Cathy Hannibal, Mark C. Jabs, Ethylin Wang